A spectrophotometric determination of the formation constants of the inclusion complexes ofα- andβ-cyclodextrins with the azonium and ammonium tautomers of methyl orange and methyl yellow
✍ Scribed by Khalid M. Tawarah; Hakam M. Abu-Shamleh
- Publisher
- Springer Netherlands
- Year
- 1991
- Tongue
- English
- Weight
- 566 KB
- Volume
- 11
- Category
- Article
- ISSN
- 0923-0750
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
The interaction of rntin and methyl-pcyclodextrin in aqueous solution was studied by UV, fluorescence spectroscopy and reversed-phase liquid chromatography. Free solution capillary electrophoresis was also used as a new means of determination. Measurements from different methods yielded the formatio
Molecular mechanics calculations were employed to study the inclusion of 2-methyl naphthoate in alpha- and beta-cyclodextrin in vacuo and in the presence of water as a solvent. The driving forces for complexation are dominated by nonbonded van der Waals host:guest interactions in both environments.
## Abstract **Summary:** Polypyrrole (PPy) microtubes with an actinomorphic morphology are synthesized by a chemical method in the presence of an inclusion complex (IC) of mono [6‐deoxy‐6‐(2‐butenedinitrile‐2,3‐dimercapto sodium salt)]‐__β__‐cyclodextrin (6‐mnt‐__β__‐CD) with methyl orange (MO) as